Canonical Allele Identifier: PA2826669754
Gene: TRMU HGNC NCBI

Linked Data

ClinVar Variation Id: 520749
ClinVar RCV Id: RCV000622398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269711.1:p.Ile110Ser
CA325175526
NM_001282782.2:c.329T>G